Ferroelectric liquid crystal (FLC) display technology holds the promise of fast switching times, a large viewing angle, and high resolution. FLCs have a spontaneous polarization whose direction is perpendicular to the layer. This spontaneous polarization plays an imperative role in the electro-optic switching of FLCs. Researchers have now developed a technique to amplify the spontaneous polarization by doping graphene into FLCs.
Researchers consider the rational combination of carbon nanotubes (CNTs) and graphene into three-dimensional hybrids an effective route to amplify the inherent physical properties at the macroscale. By in situ nitrogen doping and structural hybridization of carbon nanotubes and graphene, researchers have now successfully fabricated nitrogen-doped aligned carbon nanotube/graphene sandwiches. In this work, aligned CNTs and graphene layers were anchored to each other, constructing a sandwich-like hierarchical architecture with efficient 3D electron transfer pathways and ion diffusion channels.
As a prime example of how the integration of multiple disparate nanotechnology fields allows the realization of novel or expanded functionalities, researchers have demonstrated a multimodal sensing device which integrates the functionalities of three traditional single mode sensors. Specifically, the team fabricated a graphene-based multimodal biosensing device, capable of transducing protein binding events into optical, electrical, and mechanical signals.
Researchers have demonstrated the experimental realization of the first all-carbon optical diode that is ready for scalable integration along with being inherently broadband in operation with no restrictions on polarization or phase-matching criteria. As they show, harnessing the optical properties of graphene-based materials offers an opportunity to create the all-photonic analogs of diodes, transistors, and photonic logic gates that will one day enable construction of the first all-photonic computer.
A three-dimensional crumpled graphene-encapsulated nickel sulfide electrode is reported as a superior high-energy lithium storage material. Compared with an electrode without crumpled graphene encapsulation, the optimized electrode yields significant improvements, especially in the cycling stability and rate capability. This enhanced performance is attributed to the 3D framework providing high continuous electron pathway and more free space for charge and mass transfer, and the stabilizing effect of the crumpled graphene based stretchy shell.
Ever since its discovery in 2004, graphene has been considered a relatively stable, high surface area platform to anchor nanostructured catalyst materials for various electrochemical and photocatalytic applications. The emergence of solution-based graphene in the form of graphene oxide has enabled new wet-chemistry approaches to the creation of graphene-based nanocomposites. A new study raises questions about the long-term stability of reduced graphene oxide in an aqueous environment where hydroxyl radicals can be present as part of the photocatalytic reaction cycle.
Transparent conductive coatings pervade modern technology. They are a critical component of optoelectronic devices such as smartphone and tablet displays as well as solar cells. The search for novel transparent electrode materials with good stability, high transparency and excellent conductivity is driven by the required trade-off between transparency and conductivity. In new work, researchers now have simultaneously increased the conductivity and transparency of ultra thin graphite by lithium intercalation.
Researchers have developed a new separation membrane with 2D layered transition metal dichalcogenides (tungsten disulfide) for size-selective separation of small molecules of about 3 nm. The as-prepared WS2 membranes exhibit 5 times higher water permeance than graphene oxide membranes with similar rejection. To further improve the water permeance, they team employed ultrathin metal hydroxide nanostrands to create more fluidic channels while keeping the rejection rate of specific molecules unchanged.